NCT06569043

Brief Summary

The purpose of this clinical trial is to investigate appetite responses to 2 cereal products in healthy adults.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
120

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Oct 2024

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

August 21, 2024

Completed
2 days until next milestone

First Posted

Study publicly available on registry

August 23, 2024

Completed
2 months until next milestone

Study Start

First participant enrolled

October 20, 2024

Completed
4 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 24, 2024

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

October 24, 2024

Completed
Last Updated

January 13, 2025

Status Verified

January 1, 2025

Enrollment Period

4 days

First QC Date

August 21, 2024

Last Update Submit

January 10, 2025

Conditions

Outcome Measures

Primary Outcomes (6)

  • Visual Analogue Scale for Hunger 0-240 minutes

    Visual Analogue Scale for "how hungry are you right now?" is scored from 0-100 millimeters (mm), whereby a higher mm indicates more hunger. Comparing change from 0 minutes (baseline) to 240 minutes, whereby a lower mm change from baseline indicates a better outcome.

    240 minutes

  • Visual Analogue Scale for Fullness 0-240 minutes

    Visual Analogue Scale for "how full are you right now?" is scored from 0-100 millimeters (mm), whereby a higher mm indicates more fullness. Comparing change from 0 minutes (baseline) to 240 minutes, whereby a higher mm change from baseline indicates a better outcome.

    240 minutes

  • Visual Analogue Scale for Satiation 0-240 minutes

    Visual Analogue Scale for "how satiated are you right now?" is scored from 0-100 millimeters (mm), whereby a higher mm indicates more satiation. Comparing change from 0 minutes (baseline) to 240 minutes, whereby a higher mm change from baseline indicates a better outcome.

    240 minutes

  • Visual Analogue Scale for Desire to Eat 0-240 minutes

    Visual Analogue Scale for "how strong is your desire to eat right now?" is scored from 0-100 millimeters (mm), whereby a higher mm indicates more desire to eat. Comparing change from 0 minutes (baseline) to 240 minutes, whereby a lower mm change from baseline indicates a better outcome.

    240 minutes

  • Visual Analogue Scale for Prospective Consumption 0-240 minutes

    Visual Analogue Scale for "how much do you think you can eat right now?" is scored from 0-100 millimeters (mm), whereby a higher mm indicates more prospective consumption. Comparing change from 0 minutes (baseline) to 240 minutes, whereby a lower mm change from baseline indicates a better outcome.

    240 minutes

  • Visual Analogue Scale for Satisfaction 0-240 minutes

    Visual Analogue Scale for "how satisfied are you right now?" is scored from 0-100 millimeters (mm), whereby a higher mm indicates more satisfaction. Comparing change from 0 minutes (baseline) to 240 minutes, whereby a higher mm change from baseline indicates a better outcome.

    240 minutes

Study Arms (2)

Breakfast Bar

EXPERIMENTAL

Packaged breakfast bar available in retail stores

Other: Breakfast Bar

Control

NO INTERVENTION

No intervention (i.e., no food provided)

Interventions

Packaged breakfast bar product available in retail stores

Breakfast Bar

Eligibility Criteria

Age18 Years - 70 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Healthy adults 18-70 years
  • Habitual snack bar consumers (at least several times per month)
  • Body mass index 18.5-29.9 kg/m2 (based on self-reported weight and height)
  • Understand and willing to follow the study procedures
  • Willing to maintain habitual diet, physical activity pattern, and body weight throughout the trial
  • Willing to abstain from strenuous exercise, consuming alcoholic drinks 24 hours before the test day
  • Willing to provide informed consent to participate in the study

You may not qualify if:

  • Pregnant or lactating women, or women who are planning to become pregnant during the study
  • Known food allergies, sensitivities, or intolerance to any food or food ingredients
  • Participating in another clinical trial for food, investigational drug, nutritional supplement, or lifestyle modification
  • Taking medications that affect appetite, metabolism or blood pressure
  • Presence of acute diseases or infection
  • Presence or history of chronic diseases
  • Diagnosed with an eating disorder
  • Restraint eaters as determined by a score \>4 from the Dutch Eating Behavior Questionnaire
  • Lost or gained 5 or more pounds in the past 3-months
  • On a weight loss diet or undergoing intermittent fasting
  • COVID-19 infection within the past 3 months
  • Subjects who do not eat bar products

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Remote

Minneapolis, Minnesota, 55430, United States

Location

MeSH Terms

Conditions

Consumer Behavior

Condition Hierarchy (Ancestors)

Behavior

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
BASIC SCIENCE
Intervention Model
CROSSOVER
Sponsor Type
INDUSTRY
Responsible Party
SPONSOR

Study Record Dates

First Submitted

August 21, 2024

First Posted

August 23, 2024

Study Start

October 20, 2024

Primary Completion

October 24, 2024

Study Completion

October 24, 2024

Last Updated

January 13, 2025

Record last verified: 2025-01

Data Sharing

IPD Sharing
Will not share

Locations